Product Details

SNP ID

rs2257914

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:30152786 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AACAAGAAAATAAAACATGGTCACT[A/C]TTCCATCCCATTTCTCAGATGTCAC

Phenotype

MIM: 605701 MIM: 616976

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

TRIM10 PubMed Links

Additional Information

For this assay, SNP(s) [rs17194411] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

TRIM10

Gene Name

tripartite motif containing 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006778.3	2953	UTR 3			NP_006769.2
NM_052828.2	2953	UTR 3			NP_439893.2
XM_011514221.1	2953	UTR 3			XP_011512523.1
XM_011514222.2	2953	UTR 3			XP_011512524.1
XM_011514223.2	2953	UTR 3			XP_011512525.1
XM_011514225.1	2953	UTR 3			XP_011512527.1

Gene

TRIM40

Gene Name

tripartite motif containing 40

There are no transcripts associated with this gene.

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